Real-world treatment patterns and clinical outcomes in patients with AML in Japan who were ineligible for first-line intensive chemotherapy.


Journal

International journal of hematology
ISSN: 1865-3774
Titre abrégé: Int J Hematol
Pays: Japan
ID NLM: 9111627

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 16 11 2021
accepted: 15 03 2022
revised: 15 03 2022
pubmed: 9 4 2022
medline: 28 6 2022
entrez: 8 4 2022
Statut: ppublish

Résumé

Acute myeloid leukemia (AML) predominantly affects elderly adults, and its prognosis worsens with age. Treatment options for patients in Japan ineligible for intensive chemotherapy include cytarabine/aclarubicin ± granulocyte colony-stimulating factor (CA ± G), azacitidine (AZA), low-dose cytarabine (LDAC), targeted therapy, and best supportive care (BSC). The country's aging population and the evolving treatment landscape are contributing to a need to understand treatment pathways and associated outcomes. This retrospective chart review evaluated outcomes in patients across Japan with primary/secondary AML who were ineligible for intensive chemotherapy and began first-line treatment or BSC between 01/01/2015 and 12/31/2018. The primary endpoint was overall survival (OS); secondary endpoints included progression-free survival (PFS) and healthcare resource utilization (HRU). Of 199 patients (58% > 75 years), 121 received systemic therapy (38 CA ± G, 37 AZA, 7 LDAC, 39 other) and 78 received BSC. Median OS was 5.4, 9.2, 2.2, 3.8, and 2.2 months for CA ± G, AZA, LDAC, other systemic therapy, and BSC, respectively; median PFS was 3.4, 7.7, 1.6, 2.3, and 2.1 months, respectively. HRU rates were uniformly high, with > 80% patients hospitalized in each cohort. The poor clinical outcomes and high HRU among Japanese AML patients who are ineligible for intensive chemotherapy highlight an unmet need for novel therapies.

Identifiants

pubmed: 35394258
doi: 10.1007/s12185-022-03334-8
pii: 10.1007/s12185-022-03334-8
doi:

Substances chimiques

Cytarabine 04079A1RDZ
Azacitidine M801H13NRU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

89-101

Informations de copyright

© 2022. Japanese Society of Hematology.

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Auteurs

Chikashi Yoshida (C)

Department of Hematology, National Hospital Organization Mito Medical Center, Ibaraki-machi, Japan. c.yoshida@mitomedical.org.

Takeshi Kondo (T)

Blood Disorders Center, Aiiku Hospital, Sapporo, Japan.

Tomoki Ito (T)

First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.

Masahiro Kizaki (M)

Department of Hematology, Saitama Medical Center, Saitama Medical University, Saitama, Japan.

Kazuhiko Yamamoto (K)

Department of Hematology, Okayama City Hospital, Okayama, Japan.

Toshihiro Miyamoto (T)

Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Yasuyoshi Morita (Y)

Division of Hematology and Rheumatology, Department of Internal Medicine, Kindai University, Osaka, Japan.

Tetsuya Eto (T)

Department of Hematology, Hamanomachi Hospital, Fukuoka, Japan.

Yuna Katsuoka (Y)

Department of Hematology, Sendai Medical Center, National Hospital Organization, Sendai, Japan.

Naoki Takezako (N)

Department of Hematology, Disaster Medical Center, Tokyo, Japan.

Nobuhiko Uoshima (N)

Department of Hematology, Kyoto Second Red Cross Hospital, Kyoto, Japan.

Kazunori Imada (K)

Department of Hematology, Japanese Red Cross Osaka Hospital, Osaka, Japan.

Jun Ando (J)

Department of Hematology, Juntendo University School of Medicine, Tokyo, Japan.

Takuya Komeno (T)

Department of Hematology, National Hospital Organization Mito Medical Center, Ibaraki-machi, Japan.

Akio Mori (A)

Blood Disorders Center, Aiiku Hospital, Sapporo, Japan.

Yuichi Ishikawa (Y)

Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Atsushi Satake (A)

First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.

Junichi Watanabe (J)

Department of Hematology, Saitama Medical Center, Saitama Medical University, Saitama, Japan.

Yoshiko Kawakami (Y)

AbbVie GK, Tokyo, Japan.

Tetsuo Morita (T)

AbbVie GK, Tokyo, Japan.

Ikue Taneike (I)

AbbVie GK, Tokyo, Japan.

Masahiko Nakayama (M)

AbbVie GK, Tokyo, Japan.

Yinghui Duan (Y)

AbbVie, Inc., North Chicago, IL, USA.

Belen Garbayo Guijarro (B)

AbbVie, Inc., Madrid, Spain.

Alexander Delgado (A)

AbbVie, Inc., Singapore, Singapore.

Cynthia Llamas (C)

AbbVie, Inc., North Chicago, IL, USA.

Hitoshi Kiyoi (H)

Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

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